Tag: M.W:200-300

13395-16-9, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.13395-16-9, Name is Bis(acetylacetone)copper, molecular formula is C10H16CuO4. In a Article, authors is Sergienko£¬once mentioned of 13395-16-9

Reaction of the framework 3d-organometallosiloxanes with acetylacetone

A reaction of acetylacetone with the framework sandwich-type metallosiloxanes (MOS) of general formula [PhSiO2]6M 6[PhSiO2]6, where M = Cu, Ni, Mn, was studied by GPC, 1H and 29Si NMR spectroscopy, X-ray diffraction, elemental and functional analysis. The reaction involved replacement of the metal atoms with the hydrogen atoms and is accompanied by the formation of the corresponding chelate complexes M(acac)2. Displacement of the metal from the framework MOS leads to the destruction of molecular skeleton and formation of phenylsiloxanes containing Si-OH groups. The yield and composition of the reaction products considerably depend on the nature of the metal in [PhSiO2]6M6[ThSiO2]6. A selective substitution of the metal leads to the stereoregular hexahydroxyhexaphenylcyclohexasiloxane, [PhSiO(PH)]6, cis-isomer. The structure and composition of the crystalline hexahydroxyhexaphenylcyclohexasiloxane obtained were confirmed by 29Si NMR spectroscopy, X-ray diffraction study, and functional analysis, while its TMS derivative was studied with 1H NMR spectroscopy and GPC. Using a framework manganese phenylsiloxane as an example, a reversible character of the process has been established and an alternative synthesis of this compound from hexahydroxyhexaphenylcyclohexasiloxane and Mn(acac)2 has been accomplished for the first time.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 13395-16-9

Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

In heterogeneous catalysis, the catalyst is in a different phase from the reactants. 13395-16-9, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 13395-16-9, name is Bis(acetylacetone)copper. In an article£¬Which mentioned a new discovery about 13395-16-9

Standard enthalpies of formation and combustion of a crystalline copper complex with tetramethyltetraethylporphine

The heat of combustion of a copper complex with 2,7,12,17-tetramethyl-3,8,13,18-tetraethylporphine was measured in an isothermal liquid calorimeter with a stationary calorimetric bomb. The standard enthalpies of combustion and formation of the complex studied were calculated (DeltacH =-21694.77 ¡À 12.54 kJ/mol, DeltafH = 3796.59 ¡À 12.60 kJ/mol).

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 13395-16-9 is helpful to your research. 13395-16-9

Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

13395-16-9, Chemistry can be defined as the study of matter and the changes it undergoes. You¡¯ll sometimes hear it called the central science because it is the connection between physics and all the other sciences, starting with biology.13395-16-9, Name is Bis(acetylacetone)copper, molecular formula is C10H16CuO4, introducing its new discovery.

Highly Monodisperse Cu-Sn Alloy Nanoplates for Efficient Nitrophenol Reduction Reaction via Promotion Effect of Tin

The hexagonal copper-tin alloy (Cu-Sn) nanoplates were synthesized using a high temperature solvent method, the length of six equilateral edges of hexagonal Cu-Sn nanoplates was 23 nm, and the thickness was 13 nm. The obtained hexagonal Cu-Sn nanoplates were highly monodisperse and allowed the formation of nanoarrays arranged with long-range order. The hexagonal Cu-Sn nanoplates exhibited high catalytic activity on catalytic hydrogenation of 4-nitrophenol to 4-aminophenol. Due to the promotion effect of Sn, the apparent rate constant (ka) of hexagonal Cu-Sn nanoplates was three times that of Cu nanoparticles. The density functional theory (DFT) calculations and experimental results demonstrated that Sn could promote the coordination process of -NO2 of 4-nitrophenol with Cu-Sn nanoplates and contribute to activation of 4-nitrophenol. In addition, the hexagonal Cu-Sn nanoplates showed high stability and reusability for the reduction reaction, good adaptability in different pH and the ionic strength, and wide applicability for the degradation of methylene blue, methyl orange, and rhodamine B, even in the industrial wastewater, suggesting that the Cu-Sn nanoplates are promising catalysts in organic industry wastewater treatment.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Name is Bis(acetylacetone)copper, as a common heterocyclic compound, it belongs to copper-catalyst compound, and cas is 13395-16-9, its synthesis route is as follows.

A yellow solution of H4L (0.3mmol, 0.068g) in MeOH (5mL) was added to a green solution of Cu(acac)2 (0.30mmol, 0.079g) in dmf (20mL) which was stirred under heating at ~90C. The resulting dark green solution was refluxed for 3h and after cooled at r.t. was layered with Et2O. X-ray quality blue crystals of 1¡¤MeOH were formed after 3weeks. The identity of the crystals was confirmed by unit cell determination (a=b=17.414(1), c=16.751(1) A, alpha=beta=gamma=90, V=5079A3). The crystals were filtered off and dried under vacuum. (Yield: 0.056g, ?65%). The solid was analyzed as solvent free. C44H52Cu4N4O16 requires: C, 46.07; H, 4.57; N, 4.88. Found: C, 45.88; H, 4.54; N, 4.85%. FT-IR (KBr pellets, cm-1): 3413(br,s), 2912(w), 2873(w), 2828(w), 1625(vs), 1603(s), 1543(s), 1473(s), 1448(s), 1399(m), 1385(m), 1338(m), 1300(vs), 1254(m), 1206(m), 1160(m), 1129(m), 1083(m), 1029(s), 980(w), 936(w), 915(m), 875(m), 770(s), 683(s), 633(m), 586(m), 489(m), 454(m).

13395-16-9, In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles.,13395-16-9 ,Bis(acetylacetone)copper, other downstream synthetic routes, hurry up and to see

Reference£º
Article; Lazarou, Katerina N.; Savvidou, Aikaterini; Raptopoulou, Catherine P.; Psycharis, Vassilis; Polyhedron; vol. 152; (2018); p. 125 – 137;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

7758-99-8, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. Copper(II) sulfate pentahydrate, cas is 7758-99-8,the copper-catalyst compound, it is a common compound, a new synthetic route is introduced below.

18 g of copper sulphate and 6.75 g of sodium bromide were added to 150 ML of D. M water in a 3 necked round bottom flask. The contents of flask were heated to 76-78 C to obtain a clear solution. 6g of sodium metabisulphite was then added to it in portions and stirred for 15 min. The reaction mixture was cooled to 30 2 C. CuBr solid was filtered. To 150 g of compound of formula 2 was added 1.5 1 of acetone and 600 ml of methanol. The contents of the flask were cooled to 18-20 C. 245 ml of aqueous HBR was added to the above reaction mixture at 18-20 C in a single charge. Cool the contents of the flask to 0-2 C. 120ML of 50% w/v aqueous sodium nitrite solution was added slowly to the reaction mixture by maintaining the temperature between 0-2 C, over a period of 30 minutes. The reaction mixture was maintained for 15 minutes at 0-2 C. The temperature was raised to 20-22 C. A solution of 246g of acrylamide in 900ML of acetone was added at 22-23 C in single charge. The reaction mixture was stirred for 10 minutes at 23-24 C, 4. 6g of cuprous bromide was added in a single charge under vigorous stirring and the reaction mixture maintained for 2 hours at 30-35 C. After completion of the reaction, acetone and methanol were. distilled off completely to obtain thick liquid mass. A solution of 150 g of sodium bicarbonate in 3.0 1 of D. M water was prepared. 600ML of hexane was added to it and stirred to get a clear biphasic solution. The reaction mixture was gradually quenched into above flask containing aqueous sodium bicarbonate and hexane solution over a period of 30 minutes at 23-35 C followed by stirring for 2 hours. The product was filtered and the product cake washed with D. M. Water followed by hexane and dried. The crude product obtained was suspended in water and stirred for 1 hour at 25-30 C. The product was filtered and cake washed with D. M. Water followed by hexane. The product thus obtained was suspended in hexane and stirred for 2 hours at 35- 40C. It was filtered and washed with hexane and dried to get compound of formula 3.

The chemical industry reduces the impact on the environment during synthesis,7758-99-8,Copper(II) sulfate pentahydrate,I believe this compound will play a more active role in future production and life.

Reference£º
Patent; SUN PHARMACEUTICAL INDUSTRIES LIMITED; WO2004/108721; (2004); A1;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

13395-16-9, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. Bis(acetylacetone)copper, cas is 13395-16-9,the copper-catalyst compound, it is a common compound, a new synthetic route is introduced below.

A mixture of 1.05 g (4 mmol) Cu(AcAc)2, 0.44 g (2 mmol) Zn(OAc)2, 0.38 g (2 mmol) SnCl2, and 20 ml OLA were added into a 100 ml three-neck round-bottom reaction flask connected to a nitrogen gas cylinder. The mixture solution was always stirred vigorously in the flask purged with high pure N2 gas (99.999%), during the whole synthesis. After heated at 130 C for 30 min, the mixture solution became brownish. The brownish solution was injected with 8 ml of sulfur – OLA solution (1 M), then heated at the reaction temperature T reaction 240-280 C for 1 h. When its color changed from dark brownish into blackish, the mixture solution (or product) was cooled down to room temperature (RT) and added with 15 ml of toluene for dispersing by sonication. To washing or purifying the product, 40 ml of ethanol was firstly added to let the nanoparticles flocculate and precipitate; then precipitates of nanoparticles were collected by centrifuging at 4000 rpm for 20 min and the supernatant liquid was removed; the collected precipitates were dispersed in toluene again by sonication; then ethanol was added for precipitates, new precipitates were collected again by centrifuging. The above process was repeated for three times. The final precipitates (or CZTS nanoparticles) were divided into two parts: (1) CZTS nanoparticles dispersed in toluene to form a stable ink solution and (2) CZTS power dried in a vacuum oven.

The chemical industry reduces the impact on the environment during synthesis,13395-16-9,Bis(acetylacetone)copper,I believe this compound will play a more active role in future production and life.

Reference£º
Article; Zhou, Min; Gong, Yanmei; Xu, Jian; Fang, Gang; Xu, Qingbo; Dong, Jianfeng; Journal of Alloys and Compounds; vol. 574; (2013); p. 272 – 277;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

13395-16-9, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. Bis(acetylacetone)copper, cas is 13395-16-9,the copper-catalyst compound, it is a common compound, a new synthetic route is introduced below.

Cu(C5H7O2)2 (13.1 mg, 0.05 mmol) was solubilized in 5 mL of methanoland added to a 5 mL of methanolic solution of HL (24.0 mg,0.1 mmol). The mixture was stirred under reflux for 1 h. Dark greencrystals suitable for X-ray diffraction analysis were obtained after somedays from the mother liquor at room temperature. Yield: 22.9 mg(84.5%). Melting point: Decomposes after 260 C. Molar conductivity(1 mM, DMF): 0.35 Omega-1¡¤cm2¡¤mol-1 Elemental analysis calculated forC26H22O2N8Cu (%): C. 57.61; H. 4.09; N. 20.67. Found (%): C. 57.65; H.3.83; N. 20.64. IR bands (KBr, cm-1): nu(CeO) 1371; nu(C]N) 1580,1557; nu(NeN) 1160; rho(py) 735. ESI-MS [C26H23O2N8Cu]+ calcd./found(m/z)=542.1240, 542.1251.

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of Bis(acetylacetone)copper, 13395-16-9

Reference£º
Article; Santiago, Pedro H.O.; Santiago, Mariana B.; Martins, Carlos H.G.; Gatto, Claudia C.; Inorganica Chimica Acta; vol. 508; (2020);,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

13395-16-9, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. Bis(acetylacetone)copper, cas is 13395-16-9,the copper-catalyst compound, it is a common compound, a new synthetic route is introduced below.

General procedure: CZTS nanoparticles were synthesized at different temperatures(220-320 C) for 3 hours and for variousreaction times (2-5 hours) at 240 C, usinghigh-temperature arrested precipitation in the coordinatingsolvent, oleylamine (OLA).15 Under the reactiontime of 3 hours, the reactants for synthesis ofCZTS nanoparticles didn?t dissolve enough in OLA.

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of Bis(acetylacetone)copper, 13395-16-9

Reference£º
Article; Kim, Donguk; Kim, Minha; Shim, Joongpyo; Kim, Doyoung; Choi, Wonseok; Park, Yong Seob; Choi, Youngkwan; Lee, Jaehyeong; Journal of Nanoscience and Nanotechnology; vol. 16; 5; (2016); p. 5082 – 5086;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

13395-16-9, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. Bis(acetylacetone)copper, cas is 13395-16-9,the copper-catalyst compound, it is a common compound, a new synthetic route is introduced below.

A yellow solution of H4L (0.30mmol, 0.068g) in dmf (6mL) was added to a turquoise solution of Cu(acac)2 (0.30mmol, 0.079g) in dmf (20mL). The immediately formed green solution was refluxed for 3h and left for slow evaporation. X-ray quality blue crystals of 3¡¤1.5dmf were formed after 2months, which were filtered off and dried under vacuum. (Yield: 0.053g, ?60%). The solid was analyzed as solvent free. C44H56Cu4N4O18 requires: C, 44.67; H, 4.77; N, 4.73%. Found: C, 44.49; H, 4.74; N, 4.70. FT-IR (KBr pellets, cm-1): 3553(s), 3477(s), 3414(s), 1638(s), 1617(vs), 1578(s), 1553(s), 1533(s), 1462(w), 1413(m), 1384(m), 1355(s), 1275(s), 1189(s), 1020(s), 937(s), 782(s), 684(m), 653(w), 613(s), 480(m), 455(s).

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of Bis(acetylacetone)copper, 13395-16-9

Reference£º
Article; Lazarou, Katerina N.; Savvidou, Aikaterini; Raptopoulou, Catherine P.; Psycharis, Vassilis; Polyhedron; vol. 152; (2018); p. 125 – 137;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

7758-99-8, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. Copper(II) sulfate pentahydrate, cas is 7758-99-8,the copper-catalyst compound, it is a common compound, a new synthetic route is introduced below.

[0146] Sodium nitrite (2.35 g, 34.13mmol) solution (40 mL) was added dropwise to 4- Chloro-2-fluoro aniline (4. [5G,] 31mmol) in 170 mL HBr [AT-10C] bath temperature, then the mixture was stirred for 30 min at-10C bath temperature. In parallel, copper sulfate (10.22g, 24. [29MMOL)] and sodium bromide (3.79 g, 36. [8MMOL)] were mixed and the reaction mixture was heated at [60C] for 30 min. Then sodium sulfite (2.66g, 21. [2MMOL)] was added into this copper sulfate reaction mixture and heated for [95C] for 30 min. The reaction mixture was cooled to room temperature and solid formed was washed with water to afford white solid cuprous bromide. The diazonium salt was portion wise added into the freshly prepared cuprous bromide in 40 mL HBr [AT-10C] bath temperature and the reaction mixture was then warmed to room temperature. The reaction mixture was heated at [55C] for 20 min, cooled and then extracted with ethyl acetate three times. The combined organic layer was washed with water and saturated brine solution, dried over sodium sulfate and concentrated. The crude material was purified by column chromatography (5: 95 ethyl acetate: pet ether) to afford solid product.

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of Copper(II) sulfate pentahydrate, 7758-99-8

Reference£º
Patent; CHEMOCENTRYX, INC.; WO2003/105853; (2003); A1;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”